Canonical Allele Identifier: PA2825508862
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2911465
ClinVar RCV Id: RCV003609785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077075.1:p.Thr60Ser
CA374115060
NM_001083606.3:c.178A>T