Canonical Allele Identifier: PA098860
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177629
ClinVar RCV Id: RCV000154209 RCV000168915 RCV000462813 RCV000514376 RCV000620185 RCV000765157 RCV001170485 RCV002265629 RCV003993660
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1776Gly
CA015944
NM_000257.4:c.5326A>G