Canonical Allele Identifier: PA2573165195
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1483174
ClinVar RCV Id: RCV002003092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1672Val
CA389037130
NM_000257.4:c.5015C>T