Canonical Allele Identifier: PA2825510847
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1404536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Ala973Val
CA5138163
NM_001083606.3:c.2918C>T