Canonical Allele Identifier: PA2825111782
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137560
ClinVar RCV Id: RCV003058430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp900Val
CA389047347
NM_000257.4:c.2699A>T