Canonical Allele Identifier: PA645417500
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 228913
ClinVar RCV Id: RCV000220338 RCV000795542 RCV001187402 RCV001256697 RCV001555883
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1611Val
CA044022
NM_000257.4:c.4832C>T