ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA131911
Gene: MYH7
HGNC
NCBI
Linked Data
ClinVar Variation Id:
42953
ClinVar RCV Id:
RCV000201875
RCV000491282
RCV000529912
RCV000620264
RCV000590886
RCV000656921
RCV000758039
RCV001114182
RCV001265537
RCV003320065
RCV004534742
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000248.2:p.Asp1096Tyr
CA013546
NM_000257.4:c.3286G>T