Canonical Allele Identifier: PA1139675254
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 920573
ClinVar RCV Id: RCV001179421 RCV003117809
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1663Asp
CA389037191
NM_000257.4:c.4988C>A