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