Canonical Allele Identifier: PA2573062053
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1316514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1575Asn
CA389037773
NM_000257.4:c.4725G>C
CA389037774
NM_000257.4:c.4725G>T