Canonical Allele Identifier: PA645416701
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 263955
ClinVar RCV Id: RCV000248294 RCV002518704 RCV003995701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1107Thr
CA10587771
NM_000257.4:c.3320A>C