Canonical Allele Identifier: PA2825113013
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1802219
ClinVar RCV Id: RCV002465032 RCV003533275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1561Ser
CA389037870
NM_000257.4:c.4681G>T